Entry-Level Clinical Research Assistant

Adams Clinical, Inc.; Philadelphia (Philadelphia County); On-site; USD 30,000 - 34,000; Full time

Benefits offered by this job

401(k) matching

Employee assistance program

Flexible spending account

Health insurance

Health savings account

Life insurance

Paid time off

Parental leave

Job summary

Adams Clinical is seeking an entry-level Clinical Research Assistant to support site operations in Philadelphia. This role provides hands-on experience in patient interaction, data management, and regulatory compliance within a fast-growing trial network.

You will work under supervision to learn ICH-GCP, site SOPs, and protocol guidelines while assisting with start-up activities, participant screening, and visit coordination. Training is provided, with clear opportunities for growth.

Qualifications

• High school diploma or GED required; bachelor’s preferred.
• No prior clinical research experience required; training provided.
• Strong attention to detail, organization and communication.
• Proficiency in Microsoft Office.
• Willingness to perform phlebotomy and clinical procedures as trained.

Responsibilities

• Assist with study start-up activities and site readiness.
• Screen and schedule participants; collect basic eligibility data.
• Prepare for visits; manage lab kits and CRFs.
• Serve as participant liaison; confirm appointments and coordinate transport.
• Escort participants during visits; perform vital signs and specimen collection as trained.
• Maintain source documentation and data entry in EDC systems.
• Ensure audit readiness and support monitoring visits.

Skills

Attention to detail

Organization

Communication

Phlebotomy willingness

Education

High school diploma or GED

Bachelor’s degree preferred

Tools

Microsoft Office

Job description

Adams Clinical is seeking an entry-level Clinical Research Assistant to support site operations in Philadelphia. This role provides hands-on experience in patient interaction, data management, and regulatory compliance within a fast-growing trial network.

You will work under supervision to learn ICH-GCP, site SOPs, and protocol guidelines while assisting with start-up activities, participant screening, and visit coordination. Training is provided, with clear opportunities for growth.